VIAF

Virtual International Authority File

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Leader 00000nz a2200037n 45 0
001 WKP|Q98211807 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241020233206.0
008 241020nneanz||abbn n and d
035 ‎‡a (WKP)Q98211807‏
024 ‎‡a 0000-0002-3998-185X‏ ‎‡2 orcid‏
035 ‎‡a (OCoLC)Q98211807‏
100 0 ‎‡a José L Jiménez‏ ‎‡c researcher‏ ‎‡9 en‏
375 ‎‡a 1‏ ‎‡2 iso5218‏
400 0 ‎‡a José L Jiménez‏ ‎‡c onderzoeker‏ ‎‡9 nl‏
670 ‎‡a Author's 1,3-dipolar cycloaddition of 2-dialkylaminothioisomünchnones with aliphatic aldehydes: synthesis of beta-lactams and thiiranes, structure elucidation, and rationale for chemoselective fragmentation of cycloadducts‏
670 ‎‡a Author's A family of hydrogels based on ureido-linked aminopolyol-derived amphiphiles and bolaamphiphiles: synthesis, gelation under thermal and sonochemical stimuli, and mesomorphic characterization.‏
670 ‎‡a Author's A fully diastereoselective oxidation of a mesoionic dipole with triplet molecular oxygen‏
670 ‎‡a Author's A new model for mapping the peptide backbone: predicting proton chemical shifts in proteins.‏
670 ‎‡a Author's A new synthesis of 6-oxopyrimidinium-4-olates. Theoretical study of the regioselective cycloaddition of arylisocyanates with A 1,3-thiazolium-4-olate system‏
670 ‎‡a Author's A quantitative structure-reactivity relationship in N-acetyl oxazolidines: an electrostatic interaction controls rotamer population‏
670 ‎‡a Author's Absolute Asymmetric Synthesis under Physical Fields: Facts and Fictions‏
670 ‎‡a Author's Assessing the whole range of CuAAC mechanisms by DFT calculations--on the intermediacy of copper acetylides.‏
670 ‎‡a Author's Chiral N-acyloxazolidines: synthesis, structure, and mechanistic insights‏
670 ‎‡a Author's Computational Screening of New Orthogonal Metal-Free Dipolar Cycloadditions of Mesomeric Betaines.‏
670 ‎‡a Author's Conformation of secondary amides. A predictive algorithm that correlates DFT-calculated structures and experimental proton chemical shifts.‏
670 ‎‡a Author's Cycloaddition Chemistry of 1,3-Thiazolium-4-olate Systems. Reaction with Nitroalkenes and Interpretation of Results Using PM3 Calculations‏
670 ‎‡a Author's Diastereoselective Cycloadditions of Nitroalkenes as an Approach to the Assembly of Bicyclic Nitrogen Heterocycles‏
670 ‎‡a Author's Dissecting competitive mechanisms: thionation vs. cycloaddition in the reaction of thioisomunchnones with isothiocyanates under microwave irradiation.‏
670 ‎‡a Author's Experimental and theoretical insights regarding the cycloaddition reaction of carbohydrate-based 1,2-diaza-1,3-butadienes and acrylonitrile. A model case for the behavior of chiral azoalkenes and unsymmetric olefins.‏
670 ‎‡a Author's Exploiting synthetic chemistry with mesoionic rings: improvements achieved with thioisomünchnones‏
670 ‎‡a Author's Greener media in chemical synthesis and processing‏
670 ‎‡a Author's Mechanistic studies of 1,3-dipolar cycloadditions of bicyclic thioisomünchnones with alkenes. A computational rationale focused on donor-acceptor interactions‏
670 ‎‡a Author's Münchnone-Alkene Cycloadditions: Deviations from the FMO Theory. Theoretical Studies in the Search of the Transition State‏
670 ‎‡a Author's Novel acid-catalyzed rearrangement of tetrahydro-1,2,3,4-tetrazines: unexpected formation of glycosazones‏
670 ‎‡a Author's On the dual reactivity of a Janus-type mesoionic dipole: experiments and theoretical validation‏
670 ‎‡a Author's On the enhanced reactivity and selectivity of triazole formation in molecular flasks. A theoretical rationale‏
670 ‎‡a Author's On the Plausibility of Pseudosugar Formation in Cometary Ices and Oxygen-rich Tholins‏
670 ‎‡a Author's On the prebiotic synthesis of D-sugars catalyzed by L-peptides: assessments from first-principles calculations.‏
670 ‎‡a Author's Prebiotic-Like Condensations of Cyanamide and Glyoxal: Revisiting Intractable Biotars‏
670 ‎‡a Author's Pseudo-cyclic structures of mono- and di-azaderivatives of malondialdehydes. Synthesis and conformational disentanglement by computational analyses‏
670 ‎‡a Author's Push-pull 1,3-thiazolium-5-thiolates. Formation via concerted and stepwise pathways, and theoretical evaluation of NLO properties.‏
670 ‎‡a Author's Rethinking aromaticity in H-bonded systems. Caveats for transition structures involving hydrogen transfer and π-delocalization‏
670 ‎‡a Author's Schiff bases from D-glucosamine and aliphatic ketones.‏
670 ‎‡a Author's Stepwise cycloadditions of mesoionic systems: thionation of thioisomünchnones by isothiocyanates‏
670 ‎‡a Author's Stepwise formation of 1,3-diazolium-4-thiolates by münchnone cycloadditions: promising candidates for nonlinear optics‏
670 ‎‡a Author's Substrate-Controlled Stereodifferentiation of Tandem [4 + 2]/[3 + 2] Cycloadditions by a Vicinal Carbohydrate-Based Template‏
670 ‎‡a Author's Symmetry breaking by spontaneous crystallization--is it the most plausible source of terrestrial handedness we have long been looking for?--A reappraisal‏
670 ‎‡a Author's Tautomerism in Schiff bases. The cases of 2-hydroxy-1-naphthaldehyde and 1-hydroxy-2-naphthaldehyde investigated in solution and the solid state‏
670 ‎‡a Author's Thermal and sonochemical studies on the Diels-Alder cycloadditions of masked o-benzoquinones with furans: new insights into the reaction mechanism‏
670 ‎‡a Author's Thionation of mesoionics with isothiocyanates: evidence supporting a four-step domino process and ruling out a [2 + 2] mechanism.‏
670 ‎‡a Author's Unusual aryl migration in a mesomeric betaine in the solid and liquid state: mechanistic insights into the SNAr reaction‏
670 ‎‡a Author's What does elementary chirality have to do with neutrinos?‏
909 ‎‡a (orcid) 000000023998185x‏ ‎‡9 1‏
919 ‎‡a chiralnacyloxazolidinessynthesisstructureandmechanisticinsights‏ ‎‡A Chiral N-acyloxazolidines: synthesis, structure, and mechanistic insights‏ ‎‡9 1‏
919 ‎‡a assessingthewholerangeofcuaacmechanismsbydftcalculationsontheintermediacyofcopperacetylides‏ ‎‡A Assessing the whole range of CuAAC mechanisms by DFT calculations--on the intermediacy of copper acetylides.‏ ‎‡9 1‏
919 ‎‡a ontheplausibilityofpseudosugarformationincometaryicesandoxygenrichtholins‏ ‎‡A On the Plausibility of Pseudosugar Formation in Cometary Ices and Oxygen-rich Tholins‏ ‎‡9 1‏
919 ‎‡a conformationofsecondaryamidesapredictivealgorithmthatcorrelatesdftcalculatedstructuresandexperimentalprotonchemicalshifts‏ ‎‡A Conformation of secondary amides. A predictive algorithm that correlates DFT-calculated structures and experimental proton chemical shifts.‏ ‎‡9 1‏
919 ‎‡a pushpull13thiazolium5thiolatesformationviaconcertedandstepwisepathwaysandtheoreticalevaluationofnloproperties‏ ‎‡A Push-pull 1,3-thiazolium-5-thiolates. Formation via concerted and stepwise pathways, and theoretical evaluation of NLO properties.‏ ‎‡9 1‏
919 ‎‡a ontheenhancedreactivityandselectivityoftriazoleformationinmolecularflasksatheoreticalrationale‏ ‎‡A On the enhanced reactivity and selectivity of triazole formation in molecular flasks. A theoretical rationale‏ ‎‡9 1‏
919 ‎‡a schiffbasesfrom500glucosamineandaliphaticketones‏ ‎‡A Schiff bases from D-glucosamine and aliphatic ketones.‏ ‎‡9 1‏
919 ‎‡a stepwisecycloadditionsofmesoionicsystemsthionationofthioisomunchnonesbyisothiocyanates‏ ‎‡A Stepwise cycloadditions of mesoionic systems: thionation of thioisomünchnones by isothiocyanates‏ ‎‡9 1‏
919 ‎‡a stepwiseformationof13diazolium4thiolatesbymunchnonecycloadditionspromisingcandidatesfornonlinearoptics‏ ‎‡A Stepwise formation of 1,3-diazolium-4-thiolates by münchnone cycloadditions: promising candidates for nonlinear optics‏ ‎‡9 1‏
919 ‎‡a onthedualreactivityofajanustypemesoionicdipoleexperimentsandtheoreticalvalidation‏ ‎‡A On the dual reactivity of a Janus-type mesoionic dipole: experiments and theoretical validation‏ ‎‡9 1‏
919 ‎‡a novelacidcatalyzedrearrangementoftetrahydro1234tetrazinesunexpectedformationofglycosazones‏ ‎‡A Novel acid-catalyzed rearrangement of tetrahydro-1,2,3,4-tetrazines: unexpected formation of glycosazones‏ ‎‡9 1‏
919 ‎‡a substratecontrolledstereodifferentiationoftandemcycloadditionsbyavicinalcarbohydratebasedtemplate‏ ‎‡A Substrate-Controlled Stereodifferentiation of Tandem [4 + 2]/[3 + 2] Cycloadditions by a Vicinal Carbohydrate-Based Template‏ ‎‡9 1‏
919 ‎‡a ontheprebioticsynthesisof500sugarscatalyzedby50peptidesassessmentsfrom1principlescalculations‏ ‎‡A On the prebiotic synthesis of D-sugars catalyzed by L-peptides: assessments from first-principles calculations.‏ ‎‡9 1‏
919 ‎‡a cycloadditionchemistryof13thiazolium4olatesystemsreactionwithnitroalkenesandinterpretationofresultsusingpm3calculations‏ ‎‡A Cycloaddition Chemistry of 1,3-Thiazolium-4-olate Systems. Reaction with Nitroalkenes and Interpretation of Results Using PM3 Calculations‏ ‎‡9 1‏
919 ‎‡a absoluteasymmetricsynthesisunderphysicalfieldsfactsandfictions‏ ‎‡A Absolute Asymmetric Synthesis under Physical Fields: Facts and Fictions‏ ‎‡9 1‏
919 ‎‡a diastereoselectivecycloadditionsofnitroalkenesasanapproachtotheassemblyofbicyclicnitrogenheterocycles‏ ‎‡A Diastereoselective Cycloadditions of Nitroalkenes as an Approach to the Assembly of Bicyclic Nitrogen Heterocycles‏ ‎‡9 1‏
919 ‎‡a quantitativestructurereactivityrelationshipinnacetyloxazolidinesanelectrostaticinteractioncontrolsrotamerpopulation‏ ‎‡A A quantitative structure-reactivity relationship in N-acetyl oxazolidines: an electrostatic interaction controls rotamer population‏ ‎‡9 1‏
919 ‎‡a newsynthesisof6oxopyrimidinium4olatestheoreticalstudyoftheregioselectivecycloadditionofarylisocyanateswitha13thiazolium4olatesystem‏ ‎‡A A new synthesis of 6-oxopyrimidinium-4-olates. Theoretical study of the regioselective cycloaddition of arylisocyanates with A 1,3-thiazolium-4-olate system‏ ‎‡9 1‏
919 ‎‡a whatdoeselementarychiralityhavetodowithneutrinos‏ ‎‡A What does elementary chirality have to do with neutrinos?‏ ‎‡9 1‏
919 ‎‡a unusualarylmigrationinamesomericbetaineinthesolidandliquidstatemechanisticinsightsintothesnarreaction‏ ‎‡A Unusual aryl migration in a mesomeric betaine in the solid and liquid state: mechanistic insights into the SNAr reaction‏ ‎‡9 1‏
919 ‎‡a symmetrybreakingbyspontaneouscrystallizationisitthemostplausiblesourceofterrestrialhandednesswehavelongbeenlookingforareappraisal‏ ‎‡A Symmetry breaking by spontaneous crystallization--is it the most plausible source of terrestrial handedness we have long been looking for?--A reappraisal‏ ‎‡9 1‏
919 ‎‡a tautomerisminschiffbasesthecasesof2hydroxy1naphthaldehydeand1hydroxy2naphthaldehydeinvestigatedinsolutionandthesolidstate‏ ‎‡A Tautomerism in Schiff bases. The cases of 2-hydroxy-1-naphthaldehyde and 1-hydroxy-2-naphthaldehyde investigated in solution and the solid state‏ ‎‡9 1‏
919 ‎‡a thermalandsonochemicalstudiesonthedielsaldercycloadditionsofmaskedobenzoquinoneswithfuransnewinsightsintothereactionmechanism‏ ‎‡A Thermal and sonochemical studies on the Diels-Alder cycloadditions of masked o-benzoquinones with furans: new insights into the reaction mechanism‏ ‎‡9 1‏
919 ‎‡a dissectingcompetitivemechanismsthionationvscycloadditioninthereactionofthioisomunchnoneswithisothiocyanatesundermicrowaveirradiation‏ ‎‡A Dissecting competitive mechanisms: thionation vs. cycloaddition in the reaction of thioisomunchnones with isothiocyanates under microwave irradiation.‏ ‎‡9 1‏
919 ‎‡a computationalscreeningofneworthogonalmetalfreedipolarcycloadditionsofmesomericbetaines‏ ‎‡A Computational Screening of New Orthogonal Metal-Free Dipolar Cycloadditions of Mesomeric Betaines.‏ ‎‡9 1‏
919 ‎‡a thionationofmesoionicswithisothiocyanatesevidencesupportinga4stepdominoprocessandrulingoutamechanism‏ ‎‡A Thionation of mesoionics with isothiocyanates: evidence supporting a four-step domino process and ruling out a [2 + 2] mechanism.‏ ‎‡9 1‏
919 ‎‡a prebioticlikecondensationsofcyanamideandglyoxalrevisitingintractablebiotars‏ ‎‡A Prebiotic-Like Condensations of Cyanamide and Glyoxal: Revisiting Intractable Biotars‏ ‎‡9 1‏
919 ‎‡a newmodelformappingthepeptidebackbonepredictingprotonchemicalshiftsinproteins‏ ‎‡A A new model for mapping the peptide backbone: predicting proton chemical shifts in proteins.‏ ‎‡9 1‏
919 ‎‡a pseudocyclicstructuresofmonoand501azaderivativesofmalondialdehydessynthesisandconformationaldisentanglementbycomputationalanalyses‏ ‎‡A Pseudo-cyclic structures of mono- and di-azaderivatives of malondialdehydes. Synthesis and conformational disentanglement by computational analyses‏ ‎‡9 1‏
919 ‎‡a exploitingsyntheticchemistrywithmesoionicringsimprovementsachievedwiththioisomunchnones‏ ‎‡A Exploiting synthetic chemistry with mesoionic rings: improvements achieved with thioisomünchnones‏ ‎‡9 1‏
919 ‎‡a munchnonealkenecycloadditionsdeviationsfromthefmotheorytheoreticalstudiesinthesearchofthetransitionstate‏ ‎‡A Münchnone-Alkene Cycloadditions: Deviations from the FMO Theory. Theoretical Studies in the Search of the Transition State‏ ‎‡9 1‏
919 ‎‡a 13dipolarcycloadditionof2dialkylaminothioisomunchnoneswithaliphaticaldehydessynthesisofbetalactamsandthiiranesstructureelucidationandrationaleforchemoselectivefragmentationofcycloadducts‏ ‎‡A 1,3-dipolar cycloaddition of 2-dialkylaminothioisomünchnones with aliphatic aldehydes: synthesis of beta-lactams and thiiranes, structure elucidation, and rationale for chemoselective fragmentation of cycloadducts‏ ‎‡9 1‏
919 ‎‡a mechanisticstudiesof13dipolarcycloadditionsofbicyclicthioisomunchnoneswithalkenesacomputationalrationalefocusedondonoracceptorinteractions‏ ‎‡A Mechanistic studies of 1,3-dipolar cycloadditions of bicyclic thioisomünchnones with alkenes. A computational rationale focused on donor-acceptor interactions‏ ‎‡9 1‏
919 ‎‡a experimentalandtheoreticalinsightsregardingthecycloadditionreactionofcarbohydratebased12diaza13butadienesandacrylonitrileamodelcaseforthebehaviorofchiralazoalkenesandunsymmetricolefins‏ ‎‡A Experimental and theoretical insights regarding the cycloaddition reaction of carbohydrate-based 1,2-diaza-1,3-butadienes and acrylonitrile. A model case for the behavior of chiral azoalkenes and unsymmetric olefins.‏ ‎‡9 1‏
919 ‎‡a familyofhydrogelsbasedonureidolinkedaminopolyolderivedamphiphilesandbolaamphiphilessynthesisgelationunderthermalandsonochemicalstimuliandmesomorphiccharacterization‏ ‎‡A A family of hydrogels based on ureido-linked aminopolyol-derived amphiphiles and bolaamphiphiles: synthesis, gelation under thermal and sonochemical stimuli, and mesomorphic characterization.‏ ‎‡9 1‏
919 ‎‡a fullydiastereoselectiveoxidationofamesoionicdipolewithtripletmolecularoxygen‏ ‎‡A A fully diastereoselective oxidation of a mesoionic dipole with triplet molecular oxygen‏ ‎‡9 1‏
919 ‎‡a greenermediainchemicalsynthesisandprocessing‏ ‎‡A Greener media in chemical synthesis and processing‏ ‎‡9 1‏
919 ‎‡a rethinkingaromaticityinhbondedsystemscaveatsfortransitionstructuresinvolvinghydrogentransferandπdelocalization‏ ‎‡A Rethinking aromaticity in H-bonded systems. Caveats for transition structures involving hydrogen transfer and π-delocalization‏ ‎‡9 1‏
946 ‎‡a b‏ ‎‡9 1‏
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996 ‎‡2 DNB|1099443008‏
996 ‎‡2 LC|n 2015024521‏
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996 ‎‡2 BNE|XX6438857‏
996 ‎‡2 BNE|XX1730458‏
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996 ‎‡2 NUKAT|n 2002099907‏
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996 ‎‡2 DNB|1044974052‏
996 ‎‡2 BNF|11887158‏
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996 ‎‡2 BNC|981058610669706706‏
996 ‎‡2 LC|ns2020000361‏
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996 ‎‡2 NYNYRILM|150733‏
996 ‎‡2 DNB|171245776‏
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996 ‎‡2 SUDOC|154792756‏
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996 ‎‡2 LC|nr 99005036‏
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996 ‎‡2 ISNI|0000000060246046‏
996 ‎‡2 BNE|XX868826‏
996 ‎‡2 BNE|XX1463811‏
996 ‎‡2 LC|n 88221559‏
996 ‎‡2 ISNI|000000008379423X‏
996 ‎‡2 SUDOC|085809853‏
996 ‎‡2 LC|no2011014195‏
996 ‎‡2 LC|ns2017002252‏
996 ‎‡2 BNE|XX6451685‏
996 ‎‡2 LC|no 95035097‏
996 ‎‡2 SZ|119359057‏
996 ‎‡2 BNE|XX1153978‏
996 ‎‡2 LC|ns2021003092‏
996 ‎‡2 BNE|XX1166087‏
996 ‎‡2 DNB|1056344679‏
996 ‎‡2 ISNI|0000000061004196‏
996 ‎‡2 ISNI|0000000078758349‏
996 ‎‡2 ISNI|0000000060617169‏
996 ‎‡2 BNE|XX1067638‏
996 ‎‡2 BNE|XX4831250‏
996 ‎‡2 LC|ns2022000264‏
996 ‎‡2 BNE|XX1524861‏
996 ‎‡2 RERO|A025279728‏
996 ‎‡2 ISNI|0000000119040369‏
996 ‎‡2 ISNI|0000000040003581‏
996 ‎‡2 LC|no2017100514‏
996 ‎‡2 CAOONL|ncf11241153‏
996 ‎‡2 BNC|981058511997506706‏
996 ‎‡2 BNE|XX1649910‏
996 ‎‡2 NTA|239253442‏
996 ‎‡2 ISNI|0000000034587381‏
996 ‎‡2 ISNI|0000000418483303‏
996 ‎‡2 LC|ns2013002697‏
996 ‎‡2 BNE|XX1121862‏
996 ‎‡2 BNC|981058608190106706‏
996 ‎‡2 BNE|XX1186575‏
996 ‎‡2 BNE|XX1288518‏
996 ‎‡2 BNE|XX1720522‏
996 ‎‡2 LC|n 2021023985‏
996 ‎‡2 LC|no2022028716‏
996 ‎‡2 DNB|171390822‏
996 ‎‡2 BNE|XX1019301‏
996 ‎‡2 BNE|XX1021318‏
997 ‎‡a 0 0 lived 0 0‏ ‎‡9 1‏